SODIUM BICARBONATE

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: SODIUM BICARBONATE
Generic name: SODIUM BICARBONATE
Manufacturer: Aphena Pharma Solutions - Tennessee, LLC
Product type: HUMAN OTC DRUG
SPL set ID: 15605a6d-6c90-47d5-9d1f-f66a3f27d5fc
SPL ID: 36d1abdc-f28b-4c0d-98ea-07718706c695
Version: 1
Effective date: 2017-12-13
Source export date: 2026-10-12
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:39:43

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 21 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		part331	openfda.application_number
brand name		SODIUM BICARBONATE	openfda.brand_name
generic name		SODIUM BICARBONATE	openfda.generic_name
manufacturer name		Aphena Pharma Solutions - Tennessee, LLC	openfda.manufacturer_name
ndc	package	43353-162-80	openfda.package_ndc
ndc	package	43353-162-53	openfda.package_ndc
ndc	package	43353-162-85	openfda.package_ndc
ndc	package	43353-162-60	openfda.package_ndc
ndc	package	43353-162-94	openfda.package_ndc
ndc	package	43353-162-70	openfda.package_ndc
ndc	product	43353-162	openfda.product_ndc
ndc11	package	43353016280	derived:openfda.package_ndc
ndc11	package	43353016294	derived:openfda.package_ndc
ndc11	package	43353016253	derived:openfda.package_ndc
ndc11	package	43353016260	derived:openfda.package_ndc
ndc11	package	43353016270	derived:openfda.package_ndc
ndc11	package	43353016285	derived:openfda.package_ndc
rxcui		198861	openfda.rxcui
spl id		36d1abdc-f28b-4c0d-98ea-07718706c695	id
spl set id		15605a6d-6c90-47d5-9d1f-f66a3f27d5fc	set_id
unii		8MDF5V39QO	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings Ask a doctor or pharmacist if you are on a sodium-restricted diet. if you are taking a prescription drug. Antacids may interact with certain prescription drugs. if symptons last more than 2 weeks As with any drug, if you are pregnant or nursing a baby, seek advise of a health professional before using this product.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.